510(k) K840358 ยท KRC Tester, Electrode, Surface, Electrocardiographic
IMPEDANCE/8200 MONITOR-MODEL 8300
| Applicant | Aequitron Medical, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 30, 1984 |
| Received | Jan 26, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840358
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.